In most cereals, coding sequences account for less than 20% of the genome (Flavell et al., 1977;Barakat et al., 1997); the remaining part is composed mainly of repetitive sequences, among which microsatellites and retrotransposons are of particular importance. Retrotransposons are ubiquitous and abundant components of grass genomes, constituting a major fraction of repetitive sequences (approximately 10%-60% of the genome). In many species there is a positive correlation between the copy number of retrotransposons and genome size (Pearce et al., 1996;Vicient et al., 2001;Schulman et al., 2004). It is thought that even among individuals within one population there are differences in copy numbers of a given retrotransposon. Retrotransposons are excellent tools for detecting genetic diversity as they are major generators of genomic changes. Sequences generated from retrotransposon-based molecular markers are often more polymorphic than sequences generated from random amplified polymorphic DNA (RAPD), amplified fragment length polymorphism (AFLP), or restriction fragment length polymorphism (RFLP). Detection of inter-retrotransposon amplified polymorphisms (IRAPs) became a retrotransposon-based fingerprinting technique. IRAP markers are generated by amplification of sequences, embedded between 2 retrotransposons, using outward-facing primers annealing to long terminal repeat (LTR) target sequences. This marker system was used for the first time in barley, based on the BARE-1 retrotransposon (Kalendar et al., 1999;Vicient et al., 1999). It was also used in genetic studies of the diversity or phylogenetic relationships of Oryza L.